Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males

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Standard

Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males. / Wriedt, Emil Brink; Kielgast, Urd; Svane, Maria S.; Møller, Søren; Madsbad, Sten.

In: Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 84, No. 1, 2024, p. 16-23.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Wriedt, EB, Kielgast, U, Svane, MS, Møller, S & Madsbad, S 2024, 'Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males', Scandinavian Journal of Clinical and Laboratory Investigation, vol. 84, no. 1, pp. 16-23. https://doi.org/10.1080/00365513.2024.2306537

APA

Wriedt, E. B., Kielgast, U., Svane, M. S., Møller, S., & Madsbad, S. (2024). Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males. Scandinavian Journal of Clinical and Laboratory Investigation, 84(1), 16-23. https://doi.org/10.1080/00365513.2024.2306537

Vancouver

Wriedt EB, Kielgast U, Svane MS, Møller S, Madsbad S. Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males. Scandinavian Journal of Clinical and Laboratory Investigation. 2024;84(1):16-23. https://doi.org/10.1080/00365513.2024.2306537

Author

Wriedt, Emil Brink ; Kielgast, Urd ; Svane, Maria S. ; Møller, Søren ; Madsbad, Sten. / Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males. In: Scandinavian Journal of Clinical and Laboratory Investigation. 2024 ; Vol. 84, No. 1. pp. 16-23.

Bibtex

@article{672d9e7779e84f01bbbefa329ea6160b,
title = "Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males",
abstract = "An intravenous glucose-infusion of 0.3 g glucose per Kg body weight was administered over 1 min in nine healthy males with simultaneous blood sampling from the hepatic vein, femoral artery and a peripheral vein. Insulin secretion rates (ISR) were determined by the Eaton method and the ISEC method using C-peptide concentrations from arterial and peripheral venous blood. First phase (0–10 min), second phase (10–60 min), and total insulin secretion (0–60 min) were calculated as the incremental areas (iAUC) above baseline. The primary endpoint was first phase insulin response. The first phase insulin response in artery and venous blood did not differ with the Eaton method (p = 0.25), but was significantly greater with the ISEC method in arterial compared with venous blood (p < 0.05). The first phase insulin responses did not differ between methods in artery (p = 0.73) or venous blood (p = 0.73). The first phase responses of insulin and C-peptide were significant higher in the hepatic vein compared with those in the artery (p < 0.05) and peripheral vein (p < 0.05) but did not differ significantly between the artery compared with the peripheral vein for insulin (p = 0.09) or C-peptide (p = 0.26). Prehepatic insulin secretion rates did not differ between the Eaton and ISEC methods, but with the ISEC method the first phase insulin response was significantly greater in arterial compared with venous blood. The first phase insulin response differs when calculated from plasma insulin or C-peptide and depends on sample sites.",
keywords = "C-peptide, deconvolution, Eaton method, insulin, Insulin secretion, ISEC method",
author = "Wriedt, {Emil Brink} and Urd Kielgast and Svane, {Maria S.} and S{\o}ren M{\o}ller and Sten Madsbad",
note = "Publisher Copyright: {\textcopyright} 2024 Medisinsk Fysiologisk Forenings Forlag (MFFF).",
year = "2024",
doi = "10.1080/00365513.2024.2306537",
language = "English",
volume = "84",
pages = "16--23",
journal = "Scandinavian Journal of Clinical and Laboratory Investigation. Supplement",
issn = "0085-591X",
publisher = "Taylor & Francis",
number = "1",

}

RIS

TY - JOUR

T1 - Kinetics of insulin and C-peptide and estimation of prehepatic insulin secretion rates after intravenous glucose stimulation using arterial versus venous blood sampling in healthy males

AU - Wriedt, Emil Brink

AU - Kielgast, Urd

AU - Svane, Maria S.

AU - Møller, Søren

AU - Madsbad, Sten

N1 - Publisher Copyright: © 2024 Medisinsk Fysiologisk Forenings Forlag (MFFF).

PY - 2024

Y1 - 2024

N2 - An intravenous glucose-infusion of 0.3 g glucose per Kg body weight was administered over 1 min in nine healthy males with simultaneous blood sampling from the hepatic vein, femoral artery and a peripheral vein. Insulin secretion rates (ISR) were determined by the Eaton method and the ISEC method using C-peptide concentrations from arterial and peripheral venous blood. First phase (0–10 min), second phase (10–60 min), and total insulin secretion (0–60 min) were calculated as the incremental areas (iAUC) above baseline. The primary endpoint was first phase insulin response. The first phase insulin response in artery and venous blood did not differ with the Eaton method (p = 0.25), but was significantly greater with the ISEC method in arterial compared with venous blood (p < 0.05). The first phase insulin responses did not differ between methods in artery (p = 0.73) or venous blood (p = 0.73). The first phase responses of insulin and C-peptide were significant higher in the hepatic vein compared with those in the artery (p < 0.05) and peripheral vein (p < 0.05) but did not differ significantly between the artery compared with the peripheral vein for insulin (p = 0.09) or C-peptide (p = 0.26). Prehepatic insulin secretion rates did not differ between the Eaton and ISEC methods, but with the ISEC method the first phase insulin response was significantly greater in arterial compared with venous blood. The first phase insulin response differs when calculated from plasma insulin or C-peptide and depends on sample sites.

AB - An intravenous glucose-infusion of 0.3 g glucose per Kg body weight was administered over 1 min in nine healthy males with simultaneous blood sampling from the hepatic vein, femoral artery and a peripheral vein. Insulin secretion rates (ISR) were determined by the Eaton method and the ISEC method using C-peptide concentrations from arterial and peripheral venous blood. First phase (0–10 min), second phase (10–60 min), and total insulin secretion (0–60 min) were calculated as the incremental areas (iAUC) above baseline. The primary endpoint was first phase insulin response. The first phase insulin response in artery and venous blood did not differ with the Eaton method (p = 0.25), but was significantly greater with the ISEC method in arterial compared with venous blood (p < 0.05). The first phase insulin responses did not differ between methods in artery (p = 0.73) or venous blood (p = 0.73). The first phase responses of insulin and C-peptide were significant higher in the hepatic vein compared with those in the artery (p < 0.05) and peripheral vein (p < 0.05) but did not differ significantly between the artery compared with the peripheral vein for insulin (p = 0.09) or C-peptide (p = 0.26). Prehepatic insulin secretion rates did not differ between the Eaton and ISEC methods, but with the ISEC method the first phase insulin response was significantly greater in arterial compared with venous blood. The first phase insulin response differs when calculated from plasma insulin or C-peptide and depends on sample sites.

KW - C-peptide

KW - deconvolution

KW - Eaton method

KW - insulin

KW - Insulin secretion

KW - ISEC method

U2 - 10.1080/00365513.2024.2306537

DO - 10.1080/00365513.2024.2306537

M3 - Journal article

C2 - 38265854

AN - SCOPUS:85182990914

VL - 84

SP - 16

EP - 23

JO - Scandinavian Journal of Clinical and Laboratory Investigation. Supplement

JF - Scandinavian Journal of Clinical and Laboratory Investigation. Supplement

SN - 0085-591X

IS - 1

ER -

ID: 381785838